Method for manufacturing dye-sensitized solar cells and solar cells so produced

ABSTRACT

A dye-sensitized solar cell having a porous conductive powder layer, which layer is formed by:
         deposition of a deposit comprising metal hydride particles onto a substrate;   heating the deposit in a subsequent heating step in order to decompose the metal hydride particles to metal particles; and sinter said metal particles for forming a porous conductive powder layer.

RELATED APPLICATION DATA

This application is a continuation of U.S. patent application Ser. No. 14/350,439, filed May 21, 2014, which is a national stage entry of International Application No. PCT/EP2012/056374, filed Apr. 5, 2012 that claims priority from U.S. Provisional Patent Application No. 61/545,793 filed Oct. 11, 2011, the disclosures of which are each incorporated herein by reference in their entireties.

TECHNICAL FIELD

The invention concerns a method for producing dye-sensitized solar cells, DSC, comprising at least one electrode of a porous conductive powder layer and said DSC having improved electrical performance.

BACKGROUND OF THE INVENTION

There is an increasing demand for lower cost photovoltaic solar cells.

Dye-sensitized solar cells (DSC's) developed by M Grätzel et al are a new type of solar cells made of low-cost materials and can be manufactured by conventional printing techniques, see for example U.S. Pat. No. 5,084,365.

The conventional DSC has a few micrometer thick porous TiO₂ working electrode layer deposited onto a transparent conducting substrate. The TiO₂ working electrode comprises interconnected TiO₂ particles dyed by adsorbing dye molecules (typically a Ruthenium polypyridyl complex) on the surface of the TiO₂ particles. The transparent conducting substrate is normally a transparent conducting oxide (TCO), for example fluorine-doped tin oxide (FTO), deposited onto a glass substrate. Other types of TCO materials, such as indium tin oxide (ITO), or aluminum doped zinc oxide, or antimony doped tin oxide, are used as well.

The TCO layer serves the function as a back contact extracting photo-generated electrons from the dyed TiO₂ working electrode. The TiO₂ electrode is in contact with an electrolyte (typically containing I⁻/I₃ ⁻ ion pairs) and another transparent conducting substrate, i.e., a counter electrode. The TCO layer of the counter electrode is usually covered with a thin catalytic layer of platinum. The platinum has a strong catalytic effect, facilitating the electron transfer to the electrolyte.

The edges of the conducting substrates are usually not deposited with TiO₂ electrode material. The two conducting substrates are sealed at the edges in order to protect the DSC components against the surrounding atmosphere, and to prevent the evaporation or leakage of the DSC components inside the cell.

The incoming light passes through the TCO to create photo-generated electrons from the dyed TiO₂ working electrode. TCO has a shading effect as it absorbs parts of the incoming light thus lowering the amount of light reaching the dyed TiO₂ working electrode. Increased transparency in the TCO leads to lower conductivity and vice versa. It is not possible to have high transparency and high conductivity at the same time.

Due to the low conductivity of the transparent conducting oxide TCO, the cells must be deposited in segments or strips with gaps in between. Current collectors are deposited in the gaps to connect the segments or strips to form solar cell modules. The wider the segments the greater the electronic ohmic losses in the TCO layer because of poor TCO conductivity.

The individual cells are electrically connected in parallel or in series to enhance the DSC current or DSC voltage, respectively. The electrical connection can be made outside the cells using peripheral equipment such as cables or solders. Alternatively, the electrical connection can be made inside the cells by distributing the DSC components in such a way that the desired parallel or series connection of the cells is achieved.

The low conductivity of the transparent conductive oxide, TCO, is a problem as it limits the width of the segments. Another problem is that TCO-based glass is expensive, and the use of two TCO-based glasses in the DSC construction increases the cost even further. In order to resolve these problems, attempts have been made to exchange the TCO-based glass of the back contact by vacuum deposit of a conductive metal layer on the TiO₂ working electrode by using metal sputtering techniques. Since the deposited sputtered metal layer is electrically conductive, the TCO-based glass can be exchanged with a TCO-less glass, which is much cheaper.

In Yohei Kashiwa, Yorikazu Yoshida, and Shuzi Hayase, PHYSICS LETTERS 92, 033308 (2008)) is described electro-spraying of a tetrapod-shaped ZnO onto the TiO₂ layer followed by sputtering of titanium metal on top of the ZnO covered TiO₂ layer. The tetrapod-shaped ZnO, which was embedded in the titanium layer, was then washed away by subsequent ZnO dissolution in HCL in order to form a sufficiently porous titanium layer. The porosity of the titanium layer must be sufficient in order not to create electrolyte ion diffusion limitations with resistive losses as a consequence. Also, the dye-sensitization process can be slowed down due to diffusion problems through the titanium layer.

Yohei Kashiwa, Yorikazu Yoshida, and Shuzi Hayase, PHYSICS LETTERS 92, 033308 (2008)) and US2009314339 describe methods for increasing porosity of vacuum deposited metal layers. In US2009314339 a fine-particle layer is formed on the surface of the porous TiO₂ layer and subsequently a conductive metal film is formed on the surface of the fine-particle layer; and thereafter the fine-particle layer is removed by heating or solvent-cleaning.

Sputtering and vacuum deposition of metal layers are very expensive and slow methods that are not suitable for mass-production of large areas. It is also not possible to form layers of sufficient thickness and porosity with these methods.

Other attempts have been made to lower the internal resistance of the back contact by placing the back contact on the opposite side of the working electrode from the incident light and form the back contact as a porous metal film in contact with the working electrode.

In EP1708301 is described a dye-sensitized solar cell made by printing an alumina green sheet substrate and thereafter provide a second collector electrode by screen printing a paste containing tungsten particles to a thickness of 1 to 10 micrometer; a conductive film of a platinum-containing metalized ink is screen printed over the second collector electrode (counter electrode). A further alumina green sheet for an insulating layer is formed by screen printing an alumina slurry onto the conductive film. Onto the alumina green sheet layer a first collector electrode (back contact) is applied by screen printing the tungsten-containing paste. Thereafter, the green lamina is sintered at 1500° C. in a reducing atmosphere and then the titania electrode layer is printed on the sintered laminate and dyed and thereafter the cell is sealed.

The second collector electrode need not be a printed layer and can be exchanged by a metal substrate instead. The metal can be tungsten, titanium, nickel, platinum, gold or cupper.

The tungsten particles in the paste could be exchanged with other metals, such as titanium or nickel. A pore-forming oxide material may be included in the paste, in order to secure a porosity of 10 to 30% so that the electrolyte can be distributed in the porous material.

Screen printing of the substrate is a slow procedure which often results in defects, like pin-holes in the material, which makes it difficult to print the conductive metal layer onto the green substrate.

The printed laminae are integrally sintered at 1500° C. The high sintering temperature may be needed to achieve a sintering effect between the tungsten particles.

The high temperature apart from the heating costs also requires the cell to contain specific materials that can withstand the high temperature. Sintering at high temperature is also combined with a risk of contaminating the conductive material and thus deteriorates its conducting properties.

In WO2011096154 is described a sandwich type dye-sensitized solar cell with a porous conductive metal layer formed on a glass cloth or a glass paper substrate. The porous metal layer can be formed by sputtering or by printing a paste containing titanium particles to a thickness of 0.3 to 100 micrometer. A titania paste is printed repeatedly onto the porous conductive metal film and calcinated at 400 C until the desired thickness is achieved. A transparent resin sheet can thereafter be glued to the titania electrode. Another resin sheet is provided with a transparent conductive film having a thin layer of sputtered platinum and is arranged on the top side of the glass cloth and electrolyte is provided and the cell sealed. The fine titanium metal powder used is very expensive and the procedures for preparing the cell are complicated.

Another problem with the above solutions concerns the metal particles used for forming electrodes. Tungsten particles and titanium particles have a thin layer of oxide on the surface which impairs electrical contact between the particles.

In PCT/EP2011/067603 (not published) is shown a method for producing dye-sensitized solar cells comprising a back electrode and a counter electrode of porous conductive powder layer, where the porous conductive powder layer can be made by printing a powder of metal or metal hydride and thereafter compact the powder layer to achieve contact between the particles. The hydride particles are heat treated after compaction so as to transform the hydride to metal. A further heat treatment is optional.

The compacting step is costly and can introduce irregular zones, where the material is aggregating in unwanted ways which can cause problems when the electrolyte of the DSC shall be evenly distributed throughout the layer. This is especially pronounced for layers of metal hydride particles, which to a larger degree consist of non-conform shape particles.

DESCRIPTION OF THE INVENTION

It is an objective of the present invention to provide a cost-effective method for producing a dye-sensitized solar cell, DSC, having a porous conductive powder layer.

The porous conductive powder layer will have low electrical losses due to its low resistivity. The porosity of the porous conductive powder layer will enable ionic and dye transport through the layer.

The DSC comprising a porous conductive powder layer will have increased current-handling capability. This enables building of modules of dye-sensitized solar cells where each cell can have a larger area.

The porous conductive powder layer can have different functions in the DSC:

-   -   Back contact function. A back contact extracts electrons from         the working electrode.     -   Counter electrode function. The counter electrode transfers         electrons to the electrolyte.     -   Both the back contact and counter electrode can be porous         conductive powder layers.

A porous conductive powder layer used as a back contact is in direct electrical contact with the working electrode.

The counter electrode comprises a second porous conductive powder layer. The second porous conductive powder layer can have catalytic particles integrated in the porous conductive powder structure. Alternatively the second porous conductive layer comprises a porous conductive powder layer and a separate catalytic layer in direct contact with the porous conductive powder layer. The second porous conductive powder layer is formed in the same way as the porous conductive powder layer.

The porous conductive powder layer is formed by:

-   -   Deposition of a deposit comprising metal hydride particles onto         a substrate;         -   Heating the deposit in a subsequent heating step in order to             decompose the metal hydride particles to metal particles;             and sinter said metal particles for forming a porous             conductive powder layer.

In case the second porous conductive layer is in contact with a separate catalytic layer then the second porous conductive powder layer is formed by:

-   -   Deposition of a deposit comprising metal hydride particles onto         a catalytic layer or depositing the catalytic layer onto the         deposit comprising metal hydride particles.         -   Heating the deposit in a subsequent heating step in order to             decompose the metal hydride particles to metal particles;             and sinter said metal particles for forming a porous             conductive powder layer.

In order to minimize the cell resistance it is advantageous to deposit the catalytic layer as close as possible to the back contact layer.

The metal hydrides are brittle and the metal hydride particles have a non-spherical, irregular form. The deposit of metal hydride particles form a relatively stable layer and compaction of the layer in order to achieve inter-particle contact and mechanical stability is not necessary. In a subsequent heating step or steps the metal hydride particles are decomposed to metal particles and the metal particles are sintered to form a porous conductive powder layer. The decomposition of the metal hydride particles can take place in the same heat treatment step as the sintering or be performed in a separate step prior to the sinter heat treatment step. The sinter is preferably performed in vacuum or inert gas in order to prevent contamination of the particles.

The heat treatment temperatures sufficient for sintering between the particles to take place depend on the material used. Temperatures are normally in the range of 550-1250° C., or 550-850 C or 700-1200° C.

A first heat treatment step below the sinter temperature and above the hydride decomposition temperature in order to first release the hydrogen prior to sintering is normally made at a temperature in the range of 300-600° C. TiH₂, for example, can be preheated at 350° C.-550° C. to release a substantial amount of hydrogen before sintering.

The metal particles formed from metal hydride particles receive a non-spherical, irregular form and can be basically free from oxide on the surface. This makes the particles suitable for forming a porous conductive powder layer with excellent conductivity.

For printing the deposit various techniques known in the art can be used. Examples of printing techniques are slot die coating, gravure, screen printing, knife coating, blade coating, doctor blading, flexo printing, dip coating or spraying. The dry powder deposition can be made by for example sieving or electrostatic powder deposition.

The metal hydrides particles can be mixed with a liquid to form an ink suitable for the printing process. The particles may also be milled or otherwise treated in order to achieve a particular particle size or sizes for forming the porous conductive powder layer. Other components also in solid form may be added to the ink. The deposit for dry powder deposition may contain other components for facilitating the deposition process.

The deposit of metal hydrides can be mixed with particles of pure metals or metal alloys.

The porosity of the porous conductive powder layer is important in order to secure the passage of the electrolyte in the structure. If the electrolyte is not well distributed, the efficiency of the cell will decrease.

The porosity of the porous conductive powder layer shall preferably be between 30 to 70% or between 45 to 65%, or 40 to 60%.

The metal hydrides can be hydrides of pure metals or hydrides of metal alloys or mixtures thereof.

The resulting metal component forming the porous conductive powder layer must have a suitable corrosion resistance as to withstand the environment in the DSC.

The metal hydride is preferably a hydride of titanium or titanium alloy or mixtures thereof. Other examples are hydrides of nickel alloys, like for example Hastelloy, Incoloy, Inconel; Haynes alloy and Monel or hydrides of molybdenum, tungsten, chromium, zirconium, niobium or their alloys or mixtures thereof.

Depending on which metal is used for the porous conductive powder layer and which application method is used; the thickness of the layer can vary from around 1 micro-meter up to 100 micro-meters or from 1 micro-meter to 50 micro-meters.

The deposition can be made onto various types of substrates. The substrate can be rigid or flexible and dense or porous.

Examples of substrates are TCO-less glass, TCO-covered glass, glass, metal. Other examples of substrates are porous ceramic substrates. Examples of porous ceramic substrates are glass microfiber-based substrates, or aluminosilicate fiber based substrates or substrate comprising aluminosilicate fibres and glass fibres.

The porous ceramic substrates have several advantages as substrates since they are chemically inert, can withstand high temperatures, and are readily available and cheap and simple to handle in various process steps. The porous substrates are electrical insulators, but allowing liquids and electrolyte ions to penetrate.

The porous substrates are flexible and can be handled in the form of sheets or in the form of rolls for a continuous process.

Substrates with release function enables the formation of free-standing porous conductive powder layers which may in be integrated into the cell structure during manufacturing of the DSC. Examples of such substrates are e.g., graphite, zirconia, yttrium oxide, boron nitride or substrates equipped with a thin release layer of, for example, zirconia, yttrium oxide, boron nitride to make it possible to form free-standing porous conductive powder layers.

It is also possible to print a porous conductive powder layer onto a DSC component like a separator layer or a working electrode.

The porous conductive powder layer can be formed from a deposit comprising a catalyst thus forming a second porous conductive powder layer. Said second porous conductive powder layer is suitable as counter electrode of the DSC.

The porous conductive layer can also be in direct contact with a catalytic layer thus forming a second porous conductive powder layer. Said second porous conductive powder layer is suitable as a counter electrode of the DSC.

Deposition onto a porous substrate can be made by deposing a deposit onto both sides of a porous substrate. On one side the deposit can form a porous conductive powder layer and on the other side the deposit can form a second porous conductive powder layer. The subsequent heat treatment of the deposits can be made after deposition onto both sides of the substrate has taken place.

The back contact and counter electrode are formed by the porous conductive powder layer and the second porous conductive powder layer respectively. In order for light to reach the working electrode, a transparent substrate is placed on the side of the incident light.

There are several advantages with a DSC comprising a porous conductive powder layer and/or a second porous conductive powder layer in accordance with the present invention:

-   -   the use of metal hydrides enables the porous conductive powder         layer to be formed from relatively inexpensive materials;     -   the transformation of metal hydride particles to metal particles         with non-spherical, irregular form gives porous layers with an         evenly distributed porosity;     -   the metal particles are substantially free of oxygen and the         sinter results in a porous layer with good metal         particle-to-particle connection, thus having excellent         conductivity;     -   the porous conductive powder layers allowing for fast         electrolyte ion transport and fast dye-sensitization;     -   thicker porous conductive powder layers can be formed without         electrolyte ion transport or dye-sensitization problems;     -   highly conductive porous conductive powder layer films can be         formed allowing for the printing of wider solar cell segments;     -   printing or dry powder deposition are much faster and cheaper         than vacuum deposition techniques, such as sputtering deposition         or electron beam evaporation deposition and can be done         selectively so there is no need for expensive masking, the         layers can be printed in patterns;     -   the process for forming the porous conductive powder layers is         very flexible and a variety of substrates are available.

A reason explaining the superior conductivity when using, for example, TiH₂ particles instead of Ti particles could be that the reducing atmosphere caused by the hydrogen gas that is released during the vacuum sintering procedure efficiently removes any oxide from the surface of the titanium hydride particles.

Another possible explanation for the superior electric conductivity is that the non-spherical, irregular shaped titanium particles formed by TiH₂ based particles receives a high particle-to-particle inter-connectivity, which benefits the sinter process and thus enables the formation of a both porous and electrically conductive powder layer.

The simplicity of printing or dry powder deposition of a deposit, the inexpensive materials used and the improved conductivity of the DSC comprising the porous conductive powder layer result in a cost optimized dye sensitized solar cell with improved performance characteristics.

DETAILED DESCRIPTION OF THE INVENTION

The present invention will be further explained with reference to the following description of exemplary embodiments and accompanying drawings.

The reference to TiO₂ as working electrode is not limited to TiO₂, but could be any other material or materials suitable to form the dyed working electrode of the DSC, such as for example ZnO. Likewise, the dye can be any dye suitable for the working electrode and the electrolyte any electrolyte or solid electrolyte suitable for a DSC.

The examples below are shown with deposits comprising titanium hydride. The titanium hydride can also be a titanium alloy hydride or a mixture of titanium hydride and titanium alloy hydride.

Other metal hydrides can also be used, for example hydrides of nickel alloys, like Hastelloy, Incoloy, Inconel; Haynes alloy and Monel or hydrides of molybdenum, tungsten, chromium, niobium or their alloys or mixtures thereof.

The deposit comprising metal hydride particles can be prepared as an ink suitable for printing. The ink may comprise organic binders for, e.g. improving print quality. The binders are removed before the sinter heating step is performed.

The organic substances may be removed in a heat treatment of the deposit in reducing atmosphere such as, e.g., hydrogen atmosphere or H₂/Ar atmosphere.

For forming the second porous conductive powder layer, the deposit for printing a counter electrode may comprise a catalyst. Alternatively a solution comprising a catalyst is printed separately onto a pre-formed porous conductive powder layer. The catalyst can be catalytic amounts of platinum or other known catalysts suitable for a DSC. For example, it is possible to platinise conducting carbon powder and form a surface layer of platinum on the carbon surface. Such platinised carbon powder could be added to the ink forming the deposit for the second porous conductive powder layer to render it catalytic properties. Alternatively the porous conductive powder layer is deposited on top of a catalytic layer. An example of a catalytic layer is a porous conductive powder layer of titanium comprising platinized carbon particles.

Before deposition onto a porous substrate; it can be advantageous to first make the fibre substrate surface smoother. This can be done in various ways, for example by depositing an inert porous ceramic such as aluminosilicate, SiO₂, Al₂O₃ or some other high temperature compatible ceramic which is also chemically compatible with the DSC cell components onto the surface of the porous substrate. The porous substrate can also be made smoother by applying pressure and possibly also heat to the porous substrate, e.g. by passing the porous substrate through pressurized rollers.

A DSC can have different lay-outs. Examples of lay-outs of DSCs comprising porous conductive powder layer are shown in FIGS. 1-3. The examples are not an exhaustive list of possible DSC lay-outs.

FIG. 1—A cross section of a sandwich type DSC

FIG. 2—A cross-section of a monolithic type DSC

FIG. 3—A cross-section of a monolithic type DSC

FIGS. 4a, 4b, 4c —SEM photos of a sintered metal particle layer

FIG. 1 shows a cross-section of a sandwich type DSC. A dyed TiO₂ working electrode layer 1 is positioned on top of a substrate 2. A porous conductive powder layer 3 is positioned on top of the dyed TiO₂ working electrode layer 1. A counter electrode 4 comprising a platinized porous conductive powder layer 5 and a substrate 6 are positioned opposite to the working electrode 1. The electrolyte 7 is penetrating the porous conductive powder layer 3 and the working electrode 1 and the counter electrode 4.

The porous conductive powder layer 3 works as a back contact to the dyed TiO₂ working electrode layer 1. This means that a TCO back contact layer used in conventional DSC can be omitted and be replaced by a porous conductive powder layer. The porosity of the porous conductive powder layer 3 allows for the electrolyte 7 to penetrate and pass through the porous conductive powder layer. Photo-generated charges created in the dyed TiO₂ can be extracted by the porous conductive powder layer.

A counter electrode 4 having a second porous conductive powder layer comprising platinum catalyst is replacing a platinized TCO layer on glass in terms of both electrical conductivity and catalytic effect.

The second porous conductive powder layer in the DSC can serve the function as solely an electron conductor in the counter electrode and in such a case a separate catalytic layer must be included in the counter electrode and be in direct contact with porous conductive powder layer.

The substrate 2 on dyed TiO₂ working electrode layer 1 shall be a transparent substrate, like glass.

FIG. 2 shows a cross-section of a monolithic type DSC. A dyed TiO₂ working electrode layer 1 is shown on top of a substrate 2. A porous conductive powder layer 3 is showed on top of the dyed TiO₂ working electrode layer 1. A porous separator 8 is deposited on top of the porous conductive powder layer 3. A second porous conductive powder layer comprising a catalyst act as porous counter electrode 9 deposited on top of the separator 8. The electrolyte (not shown in FIG. 2) penetrates the counter electrode 9, the separator 8, the porous conductive powder layer 3 and the dyed TiO₂ working electrode layer 1.

The porous conductive powder layer 3 works as a back contact to the working electrode 1. This means that a TCO back contact layer used in conventional DSC can be omitted and be replaced by a porous conductive powder layer. The porosity of the porous conductive powder layer allows for electrolyte to penetrate the porous conductive powder layer and pass through the porous conductive powder layer. The photo-generated charges created in the dyed TiO₂ are extracted by the porous conductive powder layer. Since the porous conductive powder layer is electrically conductive, the need for a TCO layer for charge extraction is eliminated.

The substrate 2 below the dyed TiO₂ working electrode layer 1 shall be transparent, for example glass or plastics.

The separator 8 is a porous and chemically inert and poorly electrically conductive oxide, such as alumina, aluminosilicate, magnesia, silica, and zirconia. The separator material should also be substantially inert to the electrolyte and the dye sensitization processes. The separator layer 8 should bond well to the porous conductive powder layer 3 and provide adequate electrical insulation as well as good porosity and electrolyte permeation at minimal ohmic drop in the electrolyte. It is possible to form a separator layer by multiple depositions of chemically inert and poorly conducting layers of the same or different materials. It is also possible to form a separator layer by the deposition of alternating layers of chemically inert and poorly electrically conductive layers.

The porous counter electrode 9 can have a catalytic layer and a conducting layer. The catalytic layer is adapted to catalyse the redox reaction at the counter electrode in the cell.

FIG. 3 shows a cross-section of a monolithic type DSC. A porous conductive powder layer comprising platinum particles is deposited as porous counter electrode 9 on top of a substrate 2, a separator 8 is deposited on top of the porous counter electrode 9, a porous conductive powder layer 3 is formed on top of the separator 8, and a TiO₂ working electrode layer 1 is deposited on top of the porous conductive powder layer 3. The electrolyte (not shown in FIG. 4) is in contact with the counter electrode 9, the separator 8, the porous conductive powder layer 3, and the dyed working electrode 1.

In FIG. 3, the porous conductive powder layer 3 works as a back contact to the working electrode 1. This means that a TCO back contact layer used in conventional DSC can be omitted and be replaced by a porous conductive powder layer.

The substrate 2 on the porous counter electrode 9 can be a glass substrate or a metal substrate.

In order to produce the DCS shown in FIGS. 1 to 3 the cells are sealed and additionally, electrical connections are made so that the photo-generated current can be used in an external electrical circuit.

FIG. 4 a shows a SEM photo of a free standing porous conductive powder layer of titanium particles formed from titanium hydride. The titanium hydride based ink was deposited on a zirconia substrate and dried. Vacuum sintering was performed at 850° C. for 30 minutes. After the sintering the release properties of zirconia makes it possible to remove the porous conductive powder layer from the zirconia substrate and form a free-standing layer, which can be handled without support. As is shown in the picture the shape of the titanium particles is irregular and non-spherical. The irregular shape of the resulting titanium particles in the porous conductive powder layer, is typical for titanium hydride particles deposit.

FIG. 4b shows a free standing porous conductive powder layer of titanium particles formed from titanium hydride particles. The titanium hydride ink was deposited on a alumina substrate which was pre-deposited with a layer of boron nitride particles. Vacuum sintering was performed at 850° C. for 30 minutes. As shown in the figure flakes of boron nitride particles are sitting on top of the porous conductive powder layer of titanium.

FIG. 4c shows a free standing porous conductive powder layer of titanium particles formed from titanium hydride particles. Sintering temperature of the porous conductive powder layer was 850° C., 30 minutes. As shown in the figure, a layer of porous TiO₂ (TiO₂ particle size around 20 nm) of the working electrode is deposited on top of the porous conductive powder layer. The baking temperature of the deposited TiO₂ was 500° C., 15 minutes.

The SEM micrographs of FIGS. 4a, b and c show the structure of the sintered particles of the porous conductive powder layers having non-spherical and irregular shape titanium particles and the sharp edges of the titanium particles obtained from TiH₂ based deposit.

EXAMPLES Example 1—Porous Conductive Powder Layer on a Ceramic Substrate

An ink is prepared by mixing TiH₂ with terpineol. The ink is then bead milled for 25 minutes at 5000 RPM using 0.3 mm zirconia beads. The zirconia beads are separated from the ink by filtration. The filtered ink was then printed onto a 38 μm thick, glass microfiber based substrate and then dried at 200° C. for 5 minutes. Subsequently the coated glass microfiber substrate was vacuum sintered at 585° C. The pressure during sintering was lower than 0.0001 mbar. The resulting porous conductive powder layer is a titanium metal porous film.

Subsequently further DSC components were printed onto the porous conductive powder layer and ceramic microfiber based substrate.

A variation of example 1 is that the substrate is based on aluminosilicate fibres.

Another variation of example 1 is that the substrate comprises a mixture of aluminosilicate fiber and glass microfiber.

Another variation of example 1 is that the substrate prior to printing is passed through heated rubber coated rollers causing a smoothening of the surface of the substrate.

Another variation of example 1 is that the substrate is treated with colloidal silica before passing the substrate through rubber coated rollers.

Example 2—Porous Conductive Powder Layer Printed on a Ceramic Substrate

An ink is prepared by mixing TiH₂ with terpineol. The ink was then bead milled for 30 minutes at 4000 RPM using 0.3 mm zirconia beads. The zirconia beads were separated from the ink by filtration. The filtered ink was then printed onto a 40 μm thick, 90% porous ceramic substrate of aluminosilicate fibers and then dried at 200° C. for 5 minutes. Subsequently the coated ceramic substrate was vacuum sintered at 850° C. for 30 minutes and then cooled down to around 20° C. The pressure during sintering was lower than 0.0001 mbar. The resulting porous conductive powder layer is a titanium metal porous film. Subsequently further DSC components were printed onto the porous conductive powder layer and ceramic substrate. The thickness of the porous conductive powder layer was 16 micro-meter and the porosity 44%. The sheet resistance measured was lower than 0.5 Ohm/sq.

A variation of example 2 is that the ceramic substrate is first printed with a porous layer of TiO₂ to make the substrate surface smoother and more planar before printing the TiH₂ ink. We have found that the smoother the substrate surface before printing the TiH₂ ink the lower the porous conductive powder layer sheet resistance for a given porous conductive powder layer thickness.

Example 3—Second Porous Conductive Powder Layer with Platinum Deposited on Ceramic Substrate

An ink is prepared by mixing TiH₂ with terpineol. The ink is bead milled for 25 minutes at 5000 RPM using 0.3 mm zirconia beads. The zirconia beads are separated from the ink by filtration. The filtered ink is mixed with hexachloroplatinic acid and printed onto a 33 μm thick, porous ceramic substrate of aluminosilicate and then dried at 200° C. for 5 minutes. Subsequently the printed ceramic substrate is vacuum sintered at 585° C. and then cooled down to room temperature. The pressure during sintering was lower than 0.0001 mbar. The resulting second porous conductive powder layer comprises a titanium metal porous film with catalytic amounts of platinum.

A variation of example 3 is that the filtered ink is not mixed with hexachloroplatinic acid but that a solution of hexachloroplatinic acid is printed onto the vacuum sintered porous conductive powder layer which is then dried and then heated to decompose the deposited hexachloroplatinic acid in order to deposit platinum on the surface thus forming a second porous conductive powder layer.

Another variation of example 3 is that the filtered ink is not mixed with hexachloroplatinic acid but that the filtered ink is mixed with platinized conducting particles instead.

A variation of example 3 is that the substrate is based on glass microfiber instead of aluminosilicate fibres.

Another variation of example 3 is that the substrate is based on aluminosilicate fibre and glass microfiber.

The substrate may prior to printing be passed through heated rubber coated rollers causing a smoothening of the surface of the substrate.

Example 4—Second Porous Conductive Powder Layer with Platinum Deposited on Ceramic Substrate

An ink is prepared by mixing TiH₂ with terpineol. The ink is then bead milled for 25 minutes at 6000 RPM using 0.6 mm zirconia beads. The zirconia beads are separated from the ink by filtration. The filtered ink is mixed with hexachloroplatinic acid and printed onto a 32 μm thick, 90% porous ceramic substrate of aluminosilicate and then dried at 200° C. for 5 minutes. Subsequently the printed substrate was heat treated in vacuum and sintered at 850° C. for 30 minutes and then first cooled down to around 100° C. The pressure during sintering was lower than 0.0001 mbar. The resulting second porous conductive powder layer comprises a titanium metal porous film with catalytic amounts of platinum. The thickness of the second porous conductive powder layer was 20 micrometer and the porosity 50%. The sheet resistance was lower than 0.6 Ohm/sq.

In a variation of example 4 the filtered ink is not mixed with hexachloroplatinic acid and instead a solution of hexachloroplatinic acid is printed onto the vacuum sintered porous conductive powder layer and then dried and heated to decompose the deposited hexachloroplatinic acid in order to deposit platinum on the surface of the second porous conductive powder layer.

The ceramic substrate may first be printed with a porous layer of aluminosilicate to make the substrate surface smoother and more planar before printing the TiH₂ ink.

Example 5—Porous Conductive Powder Layer onto Double Side Printed Ceramic Substrate

An ink is prepared by mixing TiH₂ with terpineol. The ink is then bead milled for 25 minutes at 5000 RPM using 0.3 mm zirconia beads. The zirconia beads are separated from the ink by filtration. The filtered ink is mixed with platinized conducting particles and printed onto a 33 μm thick, porous glass microfiber based substrate and then dried at 200° C. for 5 minutes.

Another ink prepared by mixing TiH₂ with terpineol and bead milled and filtered is then printed onto the opposite side of the glass microfiber substrate so that the first printed layer and the second printed layer are separated by the glass microfiber substrate. The double side printed substrate was then dried at 200° C. for 5 minutes.

Subsequently the double side coated ceramic substrate was vacuum sintered at 585° C. and then allowed to cool down to room temperature. The pressure during sintering was lower than 0.0001 mbar. The resulting double sided printed substrate have a porous conductive powder layer of titanium metal on one side and a second porous conductive powder layer comprising a titanium metal with catalytic amounts of platinum on the other side.

A variation of example 5 is that a porous ceramic coating is deposited on the opposite side of the ceramic substrate prior to printing of the second porous conductive powder layer. Such a ceramic print could be useful in order to prevent electrical contact between the first and second porous conductive powder layers.

Another variation of example 5 is that the TiH₂ powder is surface treated with platinum, e.g., by thermal decomposition of a platinum salt deposited on the TiH₂ powder, before making an ink.

Another variation of example 5 is that the filtered ink is mixed with hexachloroplatinic acid instead of mixing in platinized conducting particles.

Example 6—Porous Conductive Powder Layer onto Double Side Printed Ceramic Substrate

An ink is prepared by mixing TiH₂ with terpineol. The ink is bead milled for 40 minutes at 5000 RPM using 0.3 mm zirconia beads. The zirconia beads are separated from the ink by filtration. The filtered ink is mixed with hexachloroplatinic acid and printed onto a 20 μm thick, 60% porous ceramic substrate of aluminosilicate and then dried at 200° C. for 5 minutes.

Another ink comprising TiH₂ is then printed onto the other side of the ceramic substrate and then dried at 200° C. for 5 minutes.

Subsequently the double side printed ceramic substrate was vacuum sintered at 850° C. for 30 minutes and then allowed to cool down. The pressure during sintering was lower than 0.001 mbar. The resulting double sided printed substrate have a first porous conductive powder layer comprising a titanium metal porous film one side and a second porous conductive powder layer comprising a titanium metal with catalytic amounts of platinum on porous on the other side. Sheet resistance of each porous conductive powder layer was lower than 0.3 Ohm/sq. Thickness of each layer was around 10 micrometer. Porosity of each layer was higher than 45%.

A variation of example 6 is that a porous ceramic print is printed on the opposite side of the ceramic substrate prior to the printing of the second porous conductive powder layer. Such a ceramic print could be useful in order to prevent electrical contact between the first and second porous conductive powder layer and the ceramic print could therefore be useful to prevent electrical short circuit between the first and second porous conductive powder layer.

Another variation of example 6 is that the ceramic substrate is printed with a porous ceramic on both sides before printing the TiH₂ inks.

Another variation of example 6 is that TiH₂ particles are surface treated with platinum, e.g., by thermal decomposition of a platinum salt deposited on the TiH₂ particles, before making an ink.

Example 7—DSC Based on Porous Conductive Powder Layer Double Side Printed onto Ceramic Substrate

A 20 μm thick layer of TiO₂ ink containing 20 nm particles was screen printed onto the platinum free first porous conductive powder layer side of a double side printed glass microfiber substrate produced according to example 5 or 6. The thickness of the dried TiO₂ ink layer was 1-2 μm. A second 60 μm thick layer of TiO₂ ink was printed on top of the first layer of TiO₂ and dried. A third TiO₂ layer was printed on top of the second TiO₂ layer and dried. Subsequently the TiO₂ deposited structure was subjected to heat treatment in air at 500° C. for 20 minutes. After cooling down to around 70° C., the TiO₂ deposited structure was immersed in a solution of 20 mM Z907 dye in methoxy propanol and heat treated at 70° C. for 30 minutes and subsequently rinsed in methoxy propanol. Thereafter electrolyte was added to the porous conductive powder layer double side printed ceramic substrate and the structure was sealed.

Example 8—Porous Conductive Powder Layer Deposited onto TiO₂ Working Electrode

A layer of TiO₂ ink is printed on top of a borosilicate glass substrate and then dried at 120° C. for 15 minutes. The thickness of the dried TiO₂ ink layer was around 6 μm. A second layer of TiO₂ ink was printed on top of the first layer of TiO₂ and dried. The thickness of the second dried TiO₂ ink layer was around 6 μm. Subsequently the TiO₂ deposited glass was subjected to heat treatment in air at 500° C. for 15 minutes.

An ink prepared by mixing TiH₂ with terpineol and bead milled and filtered was printed onto the deposited TiO₂ layer and then dried at 200° C. for 5 minutes. Subsequently the TiH₂ coated TiO₂ glass substrate was vacuum heated at 500° C. for 10 minutes. Subsequently the substrate was vacuum sintered at 1000° C. for 30 seconds and then allowed to cool down to around 20° C. The pr₂essure during sintering was lower than 0.001 mbar. Subsequently the structure comprising the porous conductive powder layer deposited on TiO₂ coated glass is ready to be further produced to a DSC.

Example 9—Free Standing Porous Conductive Powder Layer

An ink is prepared by mixing 8 parts by weight TiH₂ (particle size 9 micrometer) and 2 parts by weight titanium particles (particle size: 1 micrometer) with terpineol. The ink is then bead milled for 15 minutes at 6000 RPM and further bead milled for 5 minutes at 7000 RPM using 0.3 mm zirconia beads, thus mixing titanium particles with TiH₂ and forming TiH₂ particles of suitable size. The zirconia beads were then separated from the ink by filtration. The filtered ink is printed onto a ceramic substrate of zirconia and then dried at 200° C. for 5 minutes. Thereafter the printed zirconia substrate with the dry layer of TiH₂ and titanium is vacuum sintered at 850° C. for 30 minutes and then cooled down to around 20° C. The pressure during sintering was lower than 0.0001 mbar. The resulting porous conductive powder layer comprises a titanium metal porous film. The sintered porous conductive powder layer is removed from the zirconia substrate and is ready to be integrated in a DSC. The sheet resistance is lower than 0.9 Ohm/sq and the thickness 24 micrometer and porosity 51%.

Example 10—Free Standing Porous Conductive Powder Layer

An ink is prepared by mixing nickel alloy hydride particles (particle size 15 μm) with terpineol and bead milling the ink for 10 minutes at 6000 RPM using 0.3 mm zirconia beads. The zirconia beads are separated from the ink by filtration. The filtered ink is printed onto a ceramic substrate of zirconia and then dried at 200° C. for 5 minutes. Thereafter the printed zirconia substrate with the dry layer of nickel hydride particles is vacuum sintered at 750° C. for 30 minutes and then cooled down to around 20° C. The pressure during sintering was lower than 0.0001 mbar. The resulting porous conductive powder layer comprises a nickel alloy porous film. The sintered layer is removed from the zirconia substrate and is ready to be integrated in a DSC. The sheet resistance was lower than 1 Ohm/sq and the thickness 19 micrometer and porosity 58%.

Example 11—Free Standing Porous Conductive Powder Layer with Platinum

An ink is prepared by mixing TiH₂ (particle size 8 μm) with terpineol. The ink is bead milled for 25 minutes at 5000 RPM using 0.3 mm zirconia beads. The zirconia beads are separated from the ink by filtration. The filtered ink is mixed with platinized conducting particles and printed onto a ceramic substrate of zirconia and then dried at 200° C. for 5 minutes. Subsequently the printed zirconia substrate is vacuum sintered at 850° C. for 30 minutes and then cooled down to around 25° C. The pressure during sintering was lower than 0.0001 mbar. The resulting second porous conductive powder layer comprises a titanium metal porous film with catalytic amounts of platinum. The sintered layer is removed from the zirconia substrate and is ready to be integrated as a counter electrode in a DSC.

Example 12—Free Standing Porous Conductive Powder Layer

An ink is prepared by mixing TiH₂ (particle size 8 μm) with terpineol. The ink is bead milled for 15 minutes at 6000 RPM and then bead milled for 5 minutes at 7000 RPM using 0.3 mm zirconia beads, thus forming TiH₂ particles of suitable size. The zirconia beads are separated from the ink by filtration. The filtered ink is printed onto a ceramic substrate of zirconia and then dried at 200° C. for 5 minutes. Thereafter the printed zirconia substrate with the dry TiH₂ layer is vacuum sintered at 600° C. and then cooled down to around 20° C. The pressure during sintering was lower than 0.0001 mbar. The resulting layer is porous conductive powder layer of titanium. The sintered layer is removed from the zirconia substrate and is ready to be integrated in a DSC. The sheet resistance of the layer was measured lower than 0.2 Ohm/sq. The thickness of the porous conductive powder layer is 12 micrometer and the porosity 45%.

A variation of example 12 can be that the zirconia substrate is exchanged with a metal foil substrate such as, e.g., molybdenum foil which is pre-deposited with a thin layer of a non-sticking material such as, e.g., boron nitride or zirconia or yttrium oxide.

Example 13—Free Standing Porous Conductive Powder Layer with Platinum

An ink is prepared by mixing TiH₂ (particle size 8 μm) with terpineol. The ink is bead milled for 15 minutes at 6000 RPM using 0.6 mm zirconia beads. The zirconia beads are then separated from the ink by filtration. The filtered ink is mixed with hexachloroplatinic acid and printed onto a ceramic substrate of zirconia and then dried at 200° C. for 5 minutes. Subsequently the printed zirconia substrate is vacuum sintered at 900° C. for 25 minutes and then cooled down to around 20° C. The pressure during sintering was lower than 0.0001 mbar. The resulting layer is a porous conductive powder layer of titanium with catalytic amounts of platinum. The sintered layer is removed from the zirconia substrate and is ready to be integrated as a counter electrode in a DSC. The sheet resistance of the layer was lower than 0.3 Ohm/sq. The thickness of the layer was 10 micrometer and the porosity 48%.

A variation of example 13 is that the filtered ink is not mixed with hexachloroplatinic acid but that a solution of hexachloroplatinic acid is printed onto the vacuum sintered porous conductive powder layer instead and then dried and heated to decompose the deposited hexachloroplatinic acid in order to deposit platinum on the surface of the vacuum sintered porous conductive powder layer.

Example 14—DSC Based on Free Standing Porous Conductive Powder Layer

A porous conductive powder layer produced according to example 12 was immersed into a 0.02 M TiCl₄ solution in water and heat treated at 70° for 30 minutes. The layer was removed from the TiCl₄ solution and rinsed in first water and then ethanol. Subsequently a layer of TiO₂ based ink was printed on one side of the PCPL and then dried. The thickness of the dried TiO₂ ink layer was 1-2 μm. A second 60 μm thick layer of TiO₂ ink was printed on top of the first layer of TiO₂ and dried. A third TiO₂ layer was printed on top of the second TiO₂ layer and dried. Subsequently the structure was subjected to a heat treatment in air at 500° C. for 30 minutes. After allowing the structure to cool down; the structure was immersed in 0.02 M TiCl₄ in water and heat treated at 70° C. for 30 minutes. After rinsing the TiO₂ deposited PCPL in water and ethanol it was heat treated at 500° C. in air for 5 minutes. Subsequently the TiO₂ deposited porous conductive powder layer structure was immersed in a solution of 20 mM Z907 dye in methoxy-propanol and heat treated at 70° C. for 30 minutes and then rinsed in methoxy propanol. A free standing second porous conductive powder layer comprising platinum or a PCPL with platinum deposited on ceramic substrate in accordance with example 11 or 13, is positioned at a 25 μm distance from the down side of the porous conductive powder layer opposite to the dyed TiO₂ working electrode layer. Thereafter electrolyte was added and the cell sealed. The efficiency of the cell was measured at simulated AM 1.5 light. The efficiency of the cell was 8.2%.

A variation of example 14 is that one or both of the TiCl₄ treatments are omitted.

Another variation of example 14 is that the free standing second porous conductive powder layer is exchanged with a platinized titanium foil.

Another variation of example 14 is that, instead of using a free standing second porous conductive powder layer with platinum, a second porous conductive powder layer with platinum deposited on ceramic substrate according to example 3 or 4 is used as counter electrode. To avoid short circuit, the surface of the ceramic substrate opposite to the second porous conductive powder layer is brought into contact with the down side of the porous conductive powder layer opposite to the dyed TiO₂ layer.

Example 15—Porous Conductive Powder Layer on Ceramic Substrate Using Dry Powder Deposition

TiH₂ powder of a particle size <2 μm is deposited onto a zirconia ceramic substrate using dry powder deposition technique by sieving the TiH₂ powder onto the ceramic substrate. Subsequently the deposited ceramic substrate was vacuum sintered at 850° C. for 30 minutes and then allowed to cool down to around 20° C. The pressure during sintering was lower than 0.0001 mbar. Thereafter the vacuum sintered porous conductive powder layer was removed from the zirconia substrate and ready to be integrated into a DSC. The sheet resistance of the layer was lower than 0.7 Ohm/sq. The thickness of the layer was 32 micrometer and the porosity 56%.

Example 16—Porous Conductive Powder Layer onto Double Side Printed Ceramic Substrate where Second Porous Conductive Powder Layer has a Separate Catalytic Layer

An ink is prepared by mixing TiH₂ with terpineol. The ink is then bead milled for 25 minutes at 5000 RPM using 0.3 mm zirconia beads. The zirconia beads are separated from the ink by filtration. The filtered ink is mixed with platinized conducting particles and printed onto a 33 μm thick, porous glass microfiber based substrate and then dried at 200° C. for 5 minutes.

Another ink is prepared by mixing TiH₂ with terpineol. The ink is then bead milled and filtered and a second platinum free layer is then printed onto the first printed layer containing platinized conducting particles. The printed substrate was then dried at 200° C. for 5 minutes.

An ink is prepared by mixing TiH₂ with terpineol. The ink is then bead milled and filtered and a third layer is then printed onto the opposite side of the glass microfiber substrate so that the first printed layer is separated from the second printed layer and the third printed layer by the glass microfiber substrate. The double side printed substrate was then dried at 200° C. for 5 minutes.

Subsequently the double side printed ceramic substrate was vacuum sintered at 585° C. and then allowed to cool down to room temperature. The pressure during sintering was lower than 0.0001 mbar. The resulting double sided printed substrate have a porous conductive powder layer of titanium metal on one side of the glass microfiber substrate and on the other side of the glass microfiber substrate there is a second porous conductive powder layer comprising titanium metal and platinum and a third porous conductive powder layer comprising titanium metal.

In the examples the ink can be made with water as a solvent or organic solvents, such as terpenes, alcohols, glycolethers, glycol ether acetates, ketones, hydrocarbons, and aromatic solvents, may be used as well.

Binders, or other such substances, can be used to enhance the mechanical strength of the deposited particle layer before the heat treatment of the layer.

To achieve a catalytic effect in the counter electrode, it is possible to mix in platinized particles of conductive metal oxides with the metal hydride particles, such as platinized ITO, ATO, PTO, and FTO. Platinized particles of conductive metal carbides and metal nitrides can also be mixed with the metal hydride particles. Also particles of platinized carbon black or graphite can be mixed with the metal hydride particles. Platinization can be accomplished by mixing, e.g., a dissolved platinum salt like, e.g., hexachloroplatinate or platinum tetrachloride with a conducting particles and removing the solvent by evaporation and heating the mixture to a temperature high enough to decompose the platinum salt and deposit metallic platinum onto the surface of the conducting particles.

There are a number of variations possible for manufacturing the porous conductive powder layers and the DSC comprising a porous conductive powder layer in accordance with the invention and the examples represent only a part of the variations possible. 

What is claimed is:
 1. A dye-sensitized solar cell comprising a porous conductive powder stack, wherein the porous conductive powder stack comprises an electrically insulating porous separator, the electrically insulating porous separator having a first surface and a second surface respectively at opposite sides of the electrically insulating porous separator relative to a direction that traverses the porous conductive powder stack, a porous conductive powder layer back contact is arranged on the first surface of the electrically insulating porous separator, a counter electrode is arranged on the second surface of the electrically insulating porous separator, and the porous conductive powder layer back contact comprises sintered metal particles having non-spherical, irregular form.
 2. A dye-sensitized solar cell according to claim 1, wherein the sintered metal particles of the porous conductive powder layer back contact are titanium particles.
 3. A dye-sensitized solar cell according to claim 1, wherein the counter electrode is a porous conductive powder layer counter electrode comprising sintered metal particles having non-spherical, irregular form.
 4. A dye-sensitized solar cell according to claim 3, wherein the sintered metal particles of the porous conductive powder layer counter electrode are titanium particles.
 5. A dye-sensitized solar cell according to claim 1, wherein the counter electrode is a porous conductive powder layer counter electrode comprising sintered metal particles having non-spherical, irregular form, and wherein the porous conductive powder layer counter electrode comprises integrated catalytic particles.
 6. A dye-sensitized solar cell according to claim 5, wherein the catalytic particles are at least one of the materials in the group consisting of platinum, platinized carbon black and platinized graphite.
 7. A dye-sensitized solar cell according to claim 5, wherein the catalytic particles are platinized particles of at least one of the materials in the group consisting of conductive metal oxides, conductive metal carbides and conductive metal nitrides.
 8. A dye-sensitized solar cell according to claim 7, wherein the platinized particles of conductive metal oxides are at least one of the materials in the group consisting of platinized indium tin oxide (ITO), antimony-doped tin oxide (ATO), and fluorine-doped tin oxide (FTO).
 9. A dye-sensitized solar cell according to claim 1, wherein the counter electrode comprises a porous conductive powder layer counter electrode comprising sintered metal particles having non-spherical, irregular form, the counter electrode comprises a separate catalytic layer in direct contact with the porous conductive powder layer counter electrode, and the separate catalytic layer is arranged on the side of the porous conductive powder layer counter electrode that is closest to the second surface of the electrically insulating porous separator.
 10. A dye-sensitized solar cell according to claim 9, wherein the separate catalytic layer is made of titanium and platinized particles of at least one of one of the materials in the group consisting of platinum, platinized carbon black and platinized graphite.
 11. A dye-sensitized solar cell according to claim 9, wherein the separate catalytic layer comprises platinized particles of at least one of the materials in the group consisting of conductive metal oxides, conductive metal carbides and conductive metal nitrides.
 12. A dye-sensitized solar cell according to claim 11, wherein the platinized particles of conductive metal oxides are at least one of the materials in the group consisting of platinized ITO, ATO, and FTO.
 13. A dye-sensitized solar cell according to claim 1, wherein at least one of the porous conductive powder layer back contact and the counter electrode has a thickness from about 1 μm to about 100 μm.
 14. A dye-sensitized solar cell according to claim 1, wherein the electrically insulating porous separator comprises one or more of the materials in the group consisting of alumina (Al₂O₃), magnesia (MgO), zirconia (ZrO₂), silica (SiO₂), and aluminosilicate (Al₂SiO₅).
 15. A dye-sensitized solar cell according to claim 1, wherein a substrate is arranged in contact with the porous conductive powder stack, said substrate comprises one or more of the materials in the group consisting of a transparent conducting oxide (TCO)-less glass, TCO-covered glass, glass, metal and a porous ceramic.
 16. A dye-sensitized solar cell according to claim 15, wherein the porous ceramic is one or more of the materials in the group consisting of glass fibres and aluminosilicate fibres.
 17. A dye-sensitized solar cell according to claim 15, wherein the substrate is a flexible substrate.
 18. A dye-sensitized solar cell according to claim 1, wherein the porous conductive powder layer back contact has a sheet resistance <1 ohm/sq.
 19. A dye-sensitized solar cell according to claim 1, wherein a working electrode comprising TiO₂ is arranged in contact with the porous conductive powder layer back contact.
 20. A porous conductive powder stack for a dye-sensitized solar cell, wherein the porous conductive powder stack comprises an electrically insulating porous separator, the electrically insulating porous separator having a first surface and a second surface respectively at opposite sides of the electrically insulating porous separator relative to a direction that traverses the porous conductive powder stack, a porous conductive powder layer back contact is arranged on the first surface of the electrically insulating porous separator, a porous conductive powder layer counter electrode is arranged on the second surface of the electrically insulating porous separator, and the porous conductive powder layer back contact and the porous conductive powder layer counter electrode comprises sintered metal particles having non-spherical, irregular form. 